Canonical Allele Identifier: CA310148647

Gene: TNNI3

Linked Data

• dbSNP Id: rs930271158
• gnomAD v3: 19-55154517-TTC-T
• gnomAD v4: 19-55154517-TTC-T
• MyVariant Identifiers: chr19:g.55665886_55665887del (hg19) ; chr19:g.55154518_55154519del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55154519_55154520del , CM000681.2:g.55154519_55154520del	GRCh38
NC_000019.9:g.55665887_55665888del , CM000681.1:g.55665887_55665888del	GRCh37
NC_000019.8:g.60357699_60357700del	NCBI36
NG_007866.2:g.8214_8215del , LRG_432:g.8214_8215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344887.10:c.372+222_372+223del MANE Select	ENSP00000341838.5:n.372+222_372+223del
ENST00000665070.1:c.405+189_405+190del	ENSP00000499482.1:n.405+189_405+190del
ENST00000344887.9:c.372+222_372+223del	ENSP00000341838.5:n.372+222_372+223del
ENST00000585806.5:n.371+222_371+223del
ENST00000586669.5:n.380+222_380+223del
ENST00000587176.5:n.778_779del
ENST00000588882.1:c.297+222_297+223del	ENSP00000466729.1:n.297+222_297+223del
NM_000363.4:c.372+222_372+223del , LRG_432t1:c.372+222_372+223del	NP_000354.4:n.372+222_372+223del
NM_000363.5:c.372+222_372+223del MANE Select	NP_000354.4:n.372+222_372+223del